chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183259360832593609GA49GENIChomozygous110324528
183259447132594472CA56GENIChomozygous110324530
183259460532594606AT18GENIChomozygous110324532
183259539732595398GA78GENIChomozygous110324534
183259746932597469TTTTTT45GENIChomozygous129529340
183259806932598070AG53GENIChomozygous110324536
183259810832598109TC48GENIChomozygous110324538
183259813832598138TTGTTG47GENIChomozygous129529341
183259843732598437T54GENICpossibly homozygous129529342
183259852532598526AT58GENIChomozygous110324540
183260148132601482CT52GENIChomozygous110324542
183260152032601521TC62GENIChomozygous110324544
183260221632602217CT52GENIChomozygous110324546
183260354232603543CT45GENIChomozygous110324548
183260454232604542A42GENIChomozygous129529343
183260475732604757A28GENICheterozygous129529344
183260477032604771TA34GENIChomozygous119488097
183260684532606846AG50GENIChomozygous110324550
183260780232607803AC40GENIChomozygous110324552
183260785932607860GA29GENIChomozygous110324554
183260811932608120AG47GENIChomozygous110324558
183260878732608788TC38GENIChomozygous110324560